遗传性出血性毛细血管扩张症与凝血因子VIII抑制剂
Hereditary hemorrhagic telangiectasia and factor VIII inhibitor.
作者信息
Sudarshan A, Natelson E A, Gordon C
出版信息
South Med J. 1985 May;78(5):623-4. doi: 10.1097/00007611-198505000-00030.
Abstract
A patient with hereditary hemorrhagic telangiectasia manifested recurrent gastrointestinal bleeding aggravated by an acquired factor VIII inhibitor. Immunosuppressive therapy with cyclophosphamide and prednisone successfully corrected the coagulation defect.
摘要
一名患有遗传性出血性毛细血管扩张症的患者表现为反复胃肠道出血，因获得性凝血因子 VIII 抑制剂而加重。环磷酰胺和泼尼松的免疫抑制治疗成功纠正了凝血缺陷。
Zotero 插件